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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414592Generated: October 30, 2026

Chlorosuccinimide → HCID 14232130, compound

https://huagongshe.com/reaction/414592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 10559130HCID 10559130—
ReactantSodium BisulfiteHCID 23665763—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14232130HCID 1423213092.6%

Reaction Steps

To a solution of N-Methyl-N-(1H-pyrrol-1-yl)-4-pyridinamine (7.7 g) in 300 ml of anhydrous tetrahydrofuran cooled to 5° with an ice bath was added N-chlorosuccinimide (5.2 g). The reaction mixture was stirred sixty hours at ambient temperature, and thereafter additional NCS (0.9 g) was added. After stirring an additional sixteen hours at ambient temperature, the reaction mixture was stirred with an aqueous solution of sodium bisulfite and extracted with ether. The organic extract was washed with water and saturated sodium chloride and thereafter dried over anhydrous magnesium sulfate, filtered and evaporated to 9.5 g of an oil. This oil was purified by HPLC (silica, ethyl acetate) to give 4.4 g of an oil. This oil was purified by column chromatography (alumina, ether) to give 2.4 g of the desired product as an oil. This oil was dissolved in 25 ml of isopropanol, filtered, and converted to the hydrochloride salt by the addition of ethereal hydrochloric acid. The solution was diluted with 25 ml of ether and cooled. The resultant precipitate was collected and dried to give 2.5 g of crystals, mp 230°-231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792562
Source datasetuspto-grants-1988_12
ORD IDord-e1b053fc9e13480e80d9b38527af23cb
Source noteuspto-grants-1988_12